High performance blue glass

ABSTRACT

A glass composition for forming a blue colored glass is disclosed. The glass composition is made up of a base glass portion, iron oxide, and at least one first additive compound selected from Nd 2 O 3  in an amount up to 1 weight percent and/or CuO in an amount up to 0.5 weight percent. The base glass portion has the following components: SiO 2  from 66 to 75 weight percent; Na 2 O from 10 to 20 weight percent; CaO from 5 to 15 weight percent; MgO from 0 to 5 weight percent; Al 2 O 3  from 0 to 5 weight percent; B 2 O 3  from 0 to 5 weight percent; and K 2 O from 0 to 5 weight percent. The total iron in the glass composition ranges from 0.3 to 1.2 weight percent, and the glass composition has a redox ratio ranging from 0.15 to 0.65.

FIELD OF THE INVENTION

The present invention relates to glass compositions for forming a blue colored glass; especially glass compositions comprising iron oxides, neodymium oxide and/or copper oxide.

BACKGROUND

Glass is used in a variety of products ranging from buildings to automotive products. Depending on the end use of the glass, the glass will be required to have certain color and other performance properties like infrared radiation absorption, ultraviolet radiation absorption, visible light absorption, total solar energy absorption, etc.

In order to produce glass having a specific color and other performance properties, various additives are added to a base glass composition. A typical base glass composition comprises Na₂O, CaO, MgO, Al₂O₃, SiO₂ and K₂O. Typical additives to a base glass composition include compounds containing iron, cobalt, nickel, selenium, chromium, titanium, etc.

For certain commercial applications, blue colored glass having certain solar performance is required. A multitude of compositions for forming blue glass are well known to those of skill in the art. For example, U.S. Pat. No. 6,313,053 discloses a composition that yields a blue colored glass. To form the blue glass, additives such as ferric oxide (Fe₂O₃) and a reducing agent such as coal, are added to a base glass composition. The reducing agent is used to control the amount of ferrous oxide (FeO) in the composition.

Glass compositions having a lower redox ratio are generally preferred over those having a higher redox ratio because glass compositions having a lower redox ratio are easier to melt, refine, and cool, therefore generally less costly to process.

The present invention provides a novel glass composition for forming blue colored glass comprising iron oxides, neodymium oxide and/or copper oxide. The glass composition of the present invention can have an iron redox ratio of 0.15 to 0.65, for example, from 0.25 to 0.50, and solar energy blocking properties.

SUMMARY OF THE INVENTION

In one non-limiting embodiment, the present invention is a glass composition for forming a blue colored glass having a base glass portion comprising: SiO₂ from 66 to 75 weight percent, Na₂O from 10 to 20 weight percent, CaO from 5 to 15 weight percent, MgO from 0 to 5 weight percent, Al₂O₃ from 0 to 5 weight percent, B₂O₃ from 0 to 5 weight percent, and K₂O from 0 to 5 weight percent, and additives consisting essentially of: total iron from about 0.3 to 1.2 weight percent; at least one first additive compound selected from Nd₂O₃ in an amount up to 1 weight percent and/or CuO in an amount up to 0.5 weight percent; and optionally one or more second additive compounds selected from CoO, Cr₂O₃, V₂O₅, CeO₂, H₂O, SO₃, TiO₂, ZnO, MoO₃, NiO, Se, La₂O₃, WO₃, Er₂O₃, SnO₂, and MnO₂, wherein the iron redox ratio of the composition ranges from 0.15 to 0.65.

In another non-limiting embodiment, the present invention provides a method for making blue colored glass comprising: mixing a glass composition as discussed above; and melting the glass composition.

DESCRIPTION OF THE INVENTION

All numbers expressing dimensions, physical characteristics, quantities of ingredients, reaction conditions, and the like used in the specification and claims are to be understood as being modified in all instances by the term “about”. Accordingly, unless indicated to the contrary, the numerical values set forth in the following specification and claims may vary depending upon the desired properties sought to be obtained by the present invention. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Moreover, all ranges disclosed herein are to be understood to encompass any and all subranges subsumed therein. For example, a stated range of “1 to 10” should be considered to include any and all subranges between (and inclusive of) the minimum value of 1 and the maximum value of 10; that is, all subranges beginning with a minimum value of 1 or more and ending with a maximum value of 10 or less, e.g., 1 to 7.8, 3 to 4.5, 6.3 to 10.

The present invention is a glass composition for a blue colored glass. The glass composition of the present invention comprises a base glass composition and additives consisting essentially of iron oxide, at least one first additive compound selected from Nd₂O₃ and/or CuO, and optionally one or more second additive compounds, which are described below in more detail.

The components of the base glass composition are shown in the table below. Weight percent range based on Component the total weight of the composition SiO₂ 66 to 75 Na₂O 10 to 20 CaO  5 to 15 MgO 0 to 5 Al₂O₃ 0 to 5 B₂O₃ 0 to 5 K₂O 0 to 5

Additives can be added to the base glass composition to obtain the required color and/or spectral properties, such as infrared radiation absorption and ultraviolet radiation absorption. Depending on the performance requirements of the glass, the additives discussed below can be added to the base glass composition.

According to the present invention, iron oxide is added to the base glass composition. As discussed herein, iron oxide is expressed in terms of the iron oxide in the ferric state (Fe₂O₃) and the iron oxide in the ferrous state (FeO). The total amount of iron oxide present in the glass composition according to the present invention is expressed in terms of Fe₂O₃ in accordance with standard analytical practice. However, this is not meant to imply that all of the iron oxide present in the composition is in the form of Fe₂O₃. Similarly, when iron oxide is expressed in terms of FeO that does not mean all of the iron oxide present is in the form FeO.

Iron oxides can be added to a glass composition to perform several functions. Fe₂O₃ is known to those of skill in the art to be a good ultraviolet radiation absorber and a yellow colorant. FeO is known to those of skill in the art to be a good infrared radiation absorber and a blue colorant.

The term “redox ratio” is used herein to reflect the relative amounts of Fe₂O₃ and FeO in the glass composition. As used herein, “redox ratio” means the amount of iron as FeO in the composition divided by the total amount of iron in the composition expressed in terms of Fe₂O₃.

Glass compositions according to present invention have total iron ranging from 0.3 to 1.2, for example, 0.4 to 0.8 or 0.5 to 0.6 weight percent based on the total weight of the composition. The redox ratio of a glass composition according to the present invention ranges from 0.15 to 0.65, for example, 0.25 to 0.5, or 0.3 to 0.4.

In addition to iron oxide, at least one first additive compound selected from neodymium oxide (Nd₂O₃) and copper oxide (CuO) is added to the base glass composition according to the present invention. In a non-limiting embodiment of the invention, Nd₂O₃ is added to the base glass composition. Nd₂O₃ is known in the art to be a violet colorant. The amount of Nd₂O₃ in the glass composition of the present invention can range up to 1 weight percent, for example, up to 0.7 weight percent, or up to 0.25 weight percent, based on the total weight of the glass composition.

In a non-limiting embodiment of the invention, CuO is added to the base glass composition. As used herein, CuO represents both valence states of copper: cuprous, Cu⁺ and cupric, Cu²⁺. Depending on the relative amounts of cuprous and cupric present in the glass composition, the CuO will impart different properties to the final glass. Cupric is known in the art as a blue colorant and an infrared absorbing material. Cuprous is colorless in compositions according to the present invention.

The relative amounts of cuprous and cupric present in the glass composition of the invention are determined, in part, by the amount of iron oxides present, the partial pressure of O₂ in the atmosphere above the glass during the melting process, and the temperature of the glass. When iron and copper oxides are mixed together, copper is reduced and iron is oxidized due to their respective electrochemical potentials as is well known in the art. The amount of CuO in the glass composition of the present invention can be up to 0.5 weight percent, for example, up to 0.3 weight percent or up to 0.2 weight percent, based on the total weight of the composition.

In addition to the base glass composition constituents described above, iron oxides as described above, and Nd₂O₃ and/or CuO, the glass composition of the present invention can optionally include one or more of the second additive compounds described below.

In a non-limiting embodiment of the invention, cobalt (CoO) is added to the base glass composition. CoO is known in the art to be a blue colorant. The amount of CoO in the glass composition of the present invention can range up to 40 parts per million (“ppm”), for example, from 4 ppm to 30 ppm or from 5 ppm to 15 ppm.

In a non-limiting embodiment of the invention, chromium (Cr₂O₃) is added to the base glass composition. Cr₂O₃ is known to those of skill in the art to be a green colorant. It also believed that Cr₂O₃ can provide some ultraviolet radiation absorption. The amount of Cr₂O₃ in the glass composition of the present invention can range up to 100 ppm, for example, from 5 ppm to 50 ppm or from 7 ppm to 30 ppm.

In a non-limiting embodiment of the invention, vanadium (V₂O₅ ) is added to the base-glass composition. V₂O₅ is known to those of skill in the art to act as a yellow-green colorant and an absorber of both ultraviolet and infrared radiation depending on the valence state of the vanadium compound. Also, V₂O₅ can be used as a partial or complete replacement for Cr₂O₃ in the glass composition. The amount Of V₂O₅ in the glass composition of the present invention can range up to 0.1 weight percent, based on the total weight of the final glass composition.

Other second additive compounds that can be added the base glass composition are shown in the table below. These compounds are well known to those of ordinary skill in the art. Weight Percent range based on the Component total weight of the composition CeO₂ 0 to 3 TiO₂ 0 to 0.5 ZnO 0 to 0.5 MoO₃ 0 to 0.02 (0 to 200 ppm) NiO 0 to 0.001 (0 to 10 ppm) Se 0 to 0.0003 (0 to 3 ppm) La₂O₃ 0 to 0.5 WO₃ 0 to 0.5 MnO₂ 0 to 0.5 Er₂O₃ 0 to 1 SnO₂ 0 to 2

It should be appreciated that the glass compositions disclosed herein can include small amounts of other materials, for example, melting and refining aids, tramp materials or impurities.

Glasses having different color and other performance properties can be obtained by adding combinations of the additives described above to the base glass composition. For example, in a non-limiting embodiment of the invention, Fe₂O₃ can be combined with Nd₂O₃ and/or CuO to provide a blue glass having the desired spectral properties. In a non-limiting embodiment of the invention, the blue glass has a dominant wavelength up to 500 nm.

In a non-limiting embodiment, the glass composition of the present invention is produced using a conventional float glass process, which is well known to those skilled in the art. Suitable float glass processes are disclosed in U.S. Pat. Nos. 3,083,551; 3,961,930; and 4,091,156, which are hereby incorporated by reference.

In another non-limiting embodiment of the present invention, glass can be produced using a multi-stage melting operation as disclosed in U.S. Pat. Nos. 4,381,934; 4,792,536; and 4,886,539, which are hereby incorporated by reference.

If required, a stirring arrangement that is well known in the art can be employed within the melting and/or forming stages of the glass production operation to homogenize the glass in order to produce glass of the highest optical quality.

Because float glass processes involve suspending glass on molten tin, measurable amounts of tin oxide (SnO₂) can migrate into portions of the glass that are in physical contact with the molten tin during forming. Typically, a piece of glass produced by a float glass process has an SnO₂ concentration ranging from 0 to 2.0 weight percent in the first 25 microns below the surface of the glass that was in contact with the tin. Typical background levels of SnO₂ in float glass can be as high as 30 ppm. Although high concentrations of SnO₂ in about the first 10 angstroms of the glass surface can slightly increase the reflectivity of the glass surface, the overall impact of SnO₂ on the properties of glass is minimal for most applications.

In a non-limiting embodiment of the present invention, sulfur oxide (SO₃) can be added to the base glass composition. SO₃ is known to those of ordinary skill in the art to be a melting and refining aid for a soda-lime-silica glass composition. Glass produced according to the present invention can include up to 0.3 weight percent SO₃ based on the total weight of the glass.

The combination of Fe₂O₃ and SO₃ in a glass composition can impart an amber coloration in the glass which lowers luminous transmittance as discussed in U.S. Pat. No. 4,792,536. However, it is believed that the reducing conditions required to produce the coloration in float glass compositions of the type disclosed herein are limited to approximately the first 20 microns of the lower glass surface contacting the molten tin during the float forming operation, and to a lesser extent, to the exposed upper glass surface. Because the glass has a low SO₃ content and/or the limited region of the glass in which any coloration could occur, depending on the particular soda-lime-silica-lass composition, SO₃ in these surfaces essentially has little if any material effect on the glass color or spectral properties, even if the effect could be measured. More suitably, such an effect should not amount to altering the dominant wavelength of the glass more than 3 to 5 nanometers.

Iron polysulfides, such as FeSx, can also be present in the glass composition in an amount up to 10 ppm. FeSx is a byproduct of the melting process. It is believed that FeSx is formed at redox ratios above 0.50.

In a typical float glass process, water (H₂O) is added to the glass batch during processing to prevent dusting and segregation of the batch material. H₂O can be added to the batch in an amount ranging from 2 to 4 weight percent based on the total batch weight. In the final glass composition, H₂O can be present in an amount ranging up to 1,000 ppm, for example, 200 to 600 ppm, or 300 to 500 ppm.

The amount of H₂O in the final glass composition will affect the infrared absorption characteristics of the glass. More particularly, increasing the amount of H₂O in the glass composition will increase the infrared absorption. Flat glass produced by a process that uses oxyfuel firing during melting typically has a higher H₂O content than glass produced using conventional air-fuel firing. In an oxyfuel fired melting furnace, oxygen is combined with natural gas and combusted to melt the glass batch.

Glass made according to the present invention via the float process typically has a thickness ranging from about 1 millimeter to 10 millimeters.

The glass compositions according to the present invention can be used to make glass for a variety of applications, such as but not limited to, architectural applications, automotive applications, marine applications, rail applications, etc. For automotive applications, glass produced according to the present invention typically has a thickness ranging from 0.071 to 0.197 inches (1.8 to 5 mm). Such glass can be used as automobile sidelights, automobile rear windows, or at least one ply in a multiple ply arrangement. For example, the ply can be used to make an automobile windshield comprised of two annealed glass plies which are laminated together using a polyvinyl butyral interlayer. Depending on whether the glass will be used as an automobile side light or rear window, the glass can be tempered, as is well known in the art. In a multiple ply arrangement, at least a single piece of the glass can be annealed as is well known in the art.

The spectral properties of glass can change after thermal processing, such as bending and/or tempering, or prolonged exposure to ultraviolet radiation, commonly referred to as solarization. Consequently, various embodiments of the invention are initially prepared to compensate for any losses attributable to tempering and solarization. The result is a glass product having acceptable performance properties.

EXAMPLES

The present invention is illustrated by the following non-limiting examples. Tables 1 and 2 illustrate examples of glass compositions which embody the principles of the present invention. The examples in Table 1 represent computer models generated by a glass color and spectral performance computer model developed by PPG Industries, Inc. The examples in Table 2 are actual experimental laboratory melts. To prepare the melts, the following raw materials were mixed to produce a final glass weight of approximately 700 grams: cullet* 239.74 g sand 331.10 g soda ash 108.27 g limestone  28.14 g dolomite  79.80 g salt cake  2.32 g Fe₂O₃ (total iron) as required CuO as required Nd₂O₃ as required Co₃O₄ as required *The cullet used in the melts (which formed approximately 30% of the melt) included up to 0.51 wt. % total iron, 0.055 wt. % TiO₂ and 7 ppm Cr₂O₃

Reducing agents were added to the mixture as required to control redox. A portion of the raw batch material was then placed in a silica crucible in a gas fired furnace and heated to 2450° F. (1343° C.). When the batch material melted, the remaining raw materials were added to the crucible, and the crucible was held at 2450° F. (1343° C.) for 30 minutes. The molten batch was then heated and held at 2500° F. (1371° C.) for 30 minutes, 2550° F. (1399° C.) for 30 minutes, and 2600° F. (1427° C.) for 1 hour. Next, the molten glass was fitted in water, dried and reheated to 2650° F. (1454° C.) in a platinum-rhodium crucible in an electric furnace for two hours. The molten glass was then poured out of the crucible to form a slab and annealed. Samples were cut from the slab, ground and polished for analysis.

The chemical analysis of the glass compositions (except for FeO, FeSx, and Nd₂O₃) was determined using a RIGAKU 3370 X-ray fluorescence spectrophotometer. The spectral characteristics of the glass were determined on annealed samples using a Perkin-Elmer Lambda 9 UVNIS/NIR spectrophotometer prior to tempering the glass or prolonged exposure to ultraviolet radiation, which will affect the spectral properties of the glass. The FeO and FeSx content and redox were determined using the glass color and spectral performance computer model developed by PPG Industries, Inc. The content of Nd₂O₃ was based on actual batch weight.

The following are approximate amounts of the basic oxides in the experimental melts based on the batch composition: SiO₂ 72.1 wt. % Na₂O 13.6 wt. % CaO  8.8 wt. % MgO  3.8 wt. % Al₂O₃ 0.18 wt. % K₂O 0.057 wt. % 

The spectral properties shown in Tables 1 and 2 are based on a reference thickness of 0.154 inches (4.06 mm).

The following performance parameters—solar ultraviolet transmittance (SAE Tuv), solar infrared transmittance (TSIR), solar energy transmittance (SAE Tsol), visible (luminous) transmittance (LTA), solar ultraviolet transmittance (ISO Tuv)—are discussed in the Example section. The parameters were calculated as described below:

LTA was calculated using CIE Standard Illuminant “A” with a CIE 1931 Standard (2°) Observer over the wavelength range of 380 to 770 nanometers.

ISO Tuv was calculated according to ISO 9050 (1990-02-15) over the range of 280 to 380 nanometers.

SAE Tuv was calculated according to SAE J1796 (1995-05) over the wavelength range of 300 to 400 nanometers.

TSIR was calculated over the wavelength range of 775 to 2125 nanometers using the Parry Moon air mass 2.0 d solar energy distribution at 50 nanometer intervals using the Trapezoidal Rule of integration.

SAE Tsol was calculated according to SAE J1796 (1995-05) over the wavelength range of 300 to 2500 nanometers.

Glass color in terms of dominant wavelength (DW) and excitation purity (Pe), was calculated using CIE Standard Illuminant “C” with a 1931 Standard (2°) Observer, following the procedures established in ASTM E308-90. Color coordinates L*, a*, b* (CIELAB) were calculated using CIE 1964 Standard (10°) Observer over the wavelength range of 380 to 770 nanometers and CIE Standard Illuminant D65 according to the procedures established in ASTM E 308-90. TABLE 1 Data for Modeled Examples Ex. 1 Ex. 2 Ex. 3 Ex. 4 Ex. 5 Ex. 6 Component Total Iron (wt %) 0.500 0.575 0.550 0.500 0.475 0.425 Redox Ratio 0.375 0.375 0.425 0.383 0.383 0.383 CoO wt (%) 0.0015 0.0010 0.0008 0.0005 0.0008 0.0008 Cr2O3 (wt %) 0.0007 0.0007 0.0007 0.0005 0.0005 0.0005 MnO2 wt (%) 0.0020 0.0020 0.0020 CeO2 (wt %) TiO2 (wt %) 0.025 0.025 0.025 0.027 0.027 0.027 Nd2O3 (wt %) 0.2500 0.2000 0.2000 CuO (wt %) 0.1091 0.1091 0.1091 0.1100 0.2000 0.3500 FeS(x) (wt %) 0.00003 0.00003 0.00003 0.00007 0.00007 Performance Data LTA (%) 72.41 71.88 71.62 71.81 71.55 71.62 ISO Tuv (%) 35.20 32.75 35.32 35.58 36.20 37.37 SAE Tuv (%) 51.81 49.30 51.93 52.16 52.74 53.88 SAE Tsol (%) 50.17 47.37 46.19 49.67 50.13 51.46 TSIR (%) 28.28 23.95 21.54 27.19 28.38 30.94 Color Data DW (nm) 487.76 488.75 487.98 487.24 487.10 486.93 Pe (%) 7.16 7.21 8.08 7.60 7.91 8.22 D65/10 L* 89.40 89.21 89.19 89.22 89.12 89.21 a* −7.04 −7.82 −8.11 −7.39 −7.51 −7.68 b* −4.05 −3.60 −4.45 −4.42 −4.69 −4.96 Ex. 7 Ex. 8 Ex. 9 Ex. 10 Ex. 11 Component Total Iron (wt %) 0.425 0.375 0.285 0.375 0.325 Redox Ratio 0.375 0.375 0.375 0.383 0.400 CoO wt (%) 0.0020 0.0021 0.0022 0.0014 0.0017 Cr2O3 (wt %) 0.0075 0.0100 0.0150 0.0100 0.0150 MnO2 wt (%) 0.0020 0.0020 0.0020 CeO2 (wt %) TiO2 (wt %) 0.025 0.025 0.025 0.027 0.027 Nd2O3 (wt %) 0.125 0.150 CuO (wt %) 0.1100 0.2500 0.3500 0.2500 0.1100 FeS(x) (wt %) 0.00003 0.00003 0.00003 0.00007 0.00007 Performance Data LTA (%) 71.75 71.21 71.48 71.27 71.33 ISO Tuv (%) 37.95 39.41 43.23 39.96 43.29 SAE Tuv (%) 54.40 55.75 59.17 56.09 59.06 SAE Tsol (%) 52.60 53.82 57.62 53.46 55.78 TSIR (%) 33.45 36.44 43.88 35.53 39.59 Color Data DW (nm) 488.62 488.84 489.80 489.11 489.77 Pe (%) 6.70 6.99 6.52 6.87 6.13 D65/10 L* 89.02 88.81 88.89 88.86 88.77 a* −7.06 −7.48 −7.56 −7.70 −7.23 b* −3.49 −3.55 −2.96 −3.31 −2.73

TABLE 2 Data for Experimental Melts Ex. 12 Ex. 13 Ex. 14 Ex. 15 Ex. 16 Component Total Iron (wt %) 0.375 0.423 0.428 0.429 0.612 Redox Ratio 0.400 0.352 0.455 0.505 0.383 CoO (wt %) 0.0012 Cr2O3 (wt %) 0.0075 0.0008 0.0007 0.0005 0.0005 MnO2 (wt %) 0.0019 0.0018 0.0020 CeO2 (wt %) TiO2 (wt %) 0.027 0.026 0.027 0.027 0.027 Nd2O3 (wt %) 0.250 0.250 CuO (wt %) 0.1100 0.1078 0.1084 0.1091 FeS(x) (wt %) 0.00007 Performance Data LTA (%) 71.51 79.85 78.23 77.13 71.79 ISO Tuv (%) 40.76 36.77 39.40 40.91 30.83 SAE Tuv (%) 56.98 53.80 56.45 57.81 48.15 SAE Tsol (%) 53.74 56.58 52.27 50.06 46.97 TSIR (%) 34.87 34.98 27.51 23.98 22.60 Color Data DW (nm) 487.51 491.90 489.57 488.88 488.42 Pe (%) 7.13 3.88 5.74 6.67 7.51 D65/10 L* 88.98 92.43 91.98 91.61 89.25 a* −7.01 −5.71 −6.87 −7.46 −8.17 b* −4.10 −1.06 −2.60 −3.35 −3.85 Ex. 17 Ex. 18 Ex. 19 Ex. 20 Ex. 21 Component Total Iron (wt %) 0.514 0.511 0.571 0.572 0.571 Redox Ratio 0.389 0.414 0.350 0.340 0.358 CoO (wt %) 0.0015 0.0014 Cr2O3 (wt %) 0.0006 0.0006 0.0007 0.0005 0.0005 MnO2 (wt %) CeO2 (wt %) TiO2 (wt %) 0.003 0.025 0.032 0.032 0.032 Nd2O3 (wt %) 0.075 0.075 0.250 0.220 0.250 CuO (wt %) 0.1687 0.1672 0.1680 FeS(x) (wt %) Performance Data LTA (%) 72.21 72.26 72.47 72.33 72.13 ISO Tuv (%) 35.54 35.89 26.53 27.06 27.14 SAE Tuv (%) 52.94 53.32 43.04 43.59 43.64 SAE Tsol (%) 49.71 48.82 48.27 48.07 47.63 TSIR (%) 26.66 24.93 25.37 25.02 24.27 Color Data DW (nm) 486.79 486.85 490.25 490.05 489.95 Pe (%) 7.84 8.19 6.25 6.40 6.53 D65/10 L* 89.39 89.47 89.44 89.39 89.31 a* −7.03 −7.41 −8.14 −8.17 −8.27 b* −4.90 −5.08 −2.34 −2.50 −2.60

CONCLUSIONS

As illustrated by the examples above, glass compositions having certain properties can be produced according to the present invention. For example, glass melts produced according to the present invention can yield a 0.154 inch. thick glass article having an LTA of at least 70%; an ISO Tuv no more than 40.9%; an SAE Tuv no more than 57.8%; an SAE Tsol. of no more than 56.6%; and a TSIR of no more than 35%. The color of a 0.154 inches thick piece of glass according to the present invention can be characterized by a dominant wavelength (DW) between 486.8 and 491.9 nanometers and an excitation purity between 3.9% and 8.2%.

For example, computer models show 0.154 inch thick glass can be made having an LTA of at least 70%; an ISO Tuv no more than 43.3%; an SAE Tuv no more than 59.2%; an SAE Tsol of no more than 57.6%; and a TSIR of no more than 43.9%. The color of a 0.154 inches thick piece of glass according to the present invention can be characterized by a dominant wavelength (DW) between 486.9 and 489.8 nanometers and an excitation purity between 6.1% and 9.2%.

Based on the examples provided above, a 0.154 inch (4.06 mm) thick glass article formed from the glass composition of the present invention exhibits one or more of the following spectral properties: an LTA of at least 70%, for example, at least 72%; (b) an ISO Tuv of no greater than 45%, for example, no greater than 42% or no greater than 40%; (c) an SAE Tuv no greater than 60%, for example, no greater than 55% or no greater than 50%; (d) an SAE Tsol no greater than 60%, for example, no greater than 55% or no greater than 50%; and (e) a TSIR no greater than 45%, for example,. no greater than 40% or no greater than 35%. In addition, the blue colored glass of the present invention can be characterized by a dominant wavelength of no greater than 500 nanometers, for example, between 480 and 495 nanometers, or between 485 and 490 nanometers, and an excitation purity no greater than 18%, for example, no greater than 15% or no greater than 10%, at a glass thickness of 0.154 inches. The glass of the present invention can have a redox ratio ranging from 0.15 to 0.65, for example, 0.25 to 0.50, or 0.30 to 0.40.

When the glass produced according to the present invention is used in selected areas of a motor vehicle such as the windshield or front door windows, US law requires the glass to have an LTA of at least 70%. Other countries like Europe, Japan, and Australia require an LTA of at least 75%.

It will be readily appreciated by those skilled in the art that modifications can be made to the invention without departing from the concepts disclosed in the foregoing description. Such modifications are to be considered as included within the scope of the invention. Accordingly, the particular embodiments described in detail hereinabove are illustrative only and are not limiting as to the scope of the invention, which is to be given the full breadth of the appended claims and any and all equivalents thereof. 

1. A glass composition for forming a blue colored glass comprising a base glass portion comprising: a. SiO₂ from 66 to 75 weight percent; b. Na₂O from 10 to 20 weight percent; c. CaO from 5 to 15 weight percent; d. MgO from 0 to 5 weight percent; e. Al₂O₃ from 0 to 5 weight percent; f. B₂O₃ from 0 to 5 weight percent; and g. K₂O from 0 to 5 weight percent; and additives consisting essentially of: total iron from about 0.3 to 1.2 weight percent; at least one first additive compound selected from Nd₂O₃ in an amount up to 1 weight percent, CuO in an amount up to 0.5 weight percent, and combinations thereof; and optionally one or more second additive compounds selected from CoO, Cr₂O₃, V₂O₅, CeO₂, H₂O, SO₃, TiO₂, ZnO, MoO₃, NiO, Se, La₂O₃, WO₃, Er₂O₃, SnO₂, and MnO₂, wherein the redox ratio of the composition ranges from 0.15 to 0.65 and the glass has a color characterized by a dominant wavelength up to 500 nm and an excitation purity no greater than 18 percent at a thickness of 0.154 inches.
 2. The glass composition of claim 1, wherein the redox ratio ranges from 0.25 to 0.5.
 3. The glass composition of claim 2, wherein the redox ratio ranges from 0.35 to 0.40.
 4. The glass composition of claim 1, wherein the total iron ranges from 0.4 to 0.8 weight percent.
 5. The glass composition of claim 1, wherein the glass has an LTA of at least 70%, an ISO Tuv no greater than 45%, an SAE Tuv no greater than 60%, an SAE Tsol no greater than 60%, and a TSIR no greater than 45% at a thickness of 0.154 inches.
 6. The glass composition of claim 1, wherein the glass has a color characterized by a dominant wavelength up to 495 nm and an excitation purity up to 15 percent at a thickness of 0.154 inches.
 7. The glass composition of claim 5, wherein the glass has an ISO Tuv no greater than 43% at a thickness of 0.154 inches.
 8. The glass composition of claim 5, wherein the glass has an SAE Tuv no greater than 58% at a thickness of 0.154 inches.
 9. The glass composition of claim 5, wherein the glass has an SAE Tsol no greater than 57% at a thickness of 0.154 inches.
 10. The glass composition of claim 5, wherein the glass has a TSIR no greater than 35% at a thickness of 0.154 inches.
 11. The glass composition of claim 1, wherein Nd₂O₃ is present as the first additive compound.
 12. The glass composition of claim 11, wherein Nd₂O₃ is present in an amount up to 0.7 weight percent based on the total weight of the glass composition.
 13. The glass composition of claim 1, wherein CuO is present as the first additive compound.
 14. The glass composition of claim 13, wherein CuO is present in an amount up to 0.3 weight percent based on the total weight of the glass composition.
 15. The glass composition of claim 1 wherein the first additive compound comprises CuO and Nd₂O₃.
 16. The glass composition of claim 1, wherein CoO is present as a second additive compound in an amount up to 40 PPM.
 17. The glass composition of claim 1, wherein Cr₂O₃ is present as a second additive compound in an amount up to 100 PPM.
 18. The glass composition of claim 1, wherein CeO₂ is present as a second additive compound in an amount up to 3.0 weight percent based on the total weight of the glass composition.
 19. A glass composition comprising a base glass portion comprising: a. SiO₂ from 66 to 75 weight percent; b. Na₂O from 10 to 20 weight percent; c. CaO from 5 to 15 weight percent; d. MgO from 0 to 5 weight percent; e. Al₂O₃ from 0 to 5 weight percent; f. B₂O₃ from 0 to 5 weight percent; and g. K₂O from 0 to 5 weight percent; and additives consisting essentially of: total iron from about 0.3 to 1.2 weight percent; at least one first additive compound selected from the group Nd₂O₃ in an amount up to 1 weight percent, CuO in an amount up to 0.5 weight percent, and combinations thereof; and optionally one or more second additive compounds selected from CoO, Cr₂O₃, V₂O₅, CeO₂, H₂O, SO₃, TiO₂, ZnO, MoO₃, NiO, Se, La₂O₃, WO₃, Er₂O₃, SnO₂, and MnO₂, wherein the redox ratio of the composition ranges from 0.15 to 0.65, and wherein the glass composition at a thickness of 0.154 inches has an LTA of at least 70%, an ISO Tuv no greater than 45%, an SAE Tuv no greater than 60%, an SAE Tsol no greater than 60%, and a TSIR no greater than 45%.
 20. The glass composition of claim 19, wherein the glass has an ISO Tuv no greater than 43% at a thickness of 0.154 inches.
 21. The glass composition of claim 19, wherein the glass has an SAE Tuv no greater than 55% at a thickness of 0.154 inches.
 22. The glass composition of claim 19, wherein the glass has an SAE Tsol no greater than 55% at a thickness of 0.154 inches.
 23. The glass composition of claim 19, wherein the glass has a TSIR no greater than 40% at a thickness of 0.154 inches.
 24. The glass composition of claim 19, wherein the glass has a color characterized by a dominant wavelength no greater than 500 nm and an excitation purity no greater than 18 percent at a thickness of 0.154 inches.
 25. The glass composition of claim 19 wherein the redox ratio ranges from 0.25 to 0.50.
 26. The glass composition of claim 24, wherein the glass has a color characterized by a dominant wavelength up to 495 nm and an excitation purity up to 15 percent at a thickness of 0.154 inches.
 27. A glass composition comprising a base glass portion comprising: a. SiO₂ from 66 to 75 weight percent; b. Na₂O from 10 to 20 weight percent; c. CaO from 5 to 15 weight percent; d. MgO from 0 to 5 weight percent; e. Al₂O₃ from 0 to 5 weight percent; f. B₂O₃ from 0 to 5 weight percent; and g. K₂O from 0 to 5 weight percent; and additives consisting essentially of: total iron from about 0.3 to 1.2 weight percent; and at least one first additive compound selected from Nd₂O₃ in an amount up to 1 weight percent, CuO in an amount up to 0.5 weight percent, and combinations thereof, wherein the redox ratio of the composition ranges from 0.15 to 0.65 and the glass composition has an LTA of at least 70%, an ISO Tuv no greater than 45%, an SAE Tuv no greater than 60%, an SAE Tsol no greater than 60%, and a TSIR no greater than 45% at a thickness of 0.154 inches.
 28. A glass composition according to claim 27, wherein the glass has a color characterized by a dominant wavelength no greater than 500 nm and an excitation purity no greater than 18 percent at a thickness of 0.154 inches.
 29. A method for making blue colored glass comprising a. mixing a glass composition according to claim 1; and b. melting the glass composition.
 30. The method of claim 29, wherein the made glass comprises at least one piece of glass in an automobile windshield.
 31. The method of claim 29, wherein the made glass comprises at least one piece of glass in an architectural structure. 